Synfacts 2006(3): 0255-0255  
DOI: 10.1055/s-2006-931947
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Enantioselective Alkylative Ring Opening of Heterobicyclic Alkenes via Fesulphos Ligands

Contributor(s): Mark Lautens, Andrew Martins
S. Cabrera, R. Gómez Arrayás, I. Alonso, J. C. Carretero*
Universidad Autónoma de Madrid, Spain
Further Information

Publication History

Publication Date:
21 February 2006 (online)

Significance

The enantioselective ring opening of meso heterobicyclic alkenes is a useful reaction which can give fast access to chiral, heteroatom-containing products. Although the enantioselective alkylative ring opening of heterobicyclic alkenes is known, development of new ligands can allow problematic cases to be improved. The family of Fesulphos ligands were found to be highly effective in the addition of dialkylzinc reagents to a variety of oxa- and azabicyclic alkenes. Yields are generally good, and enantiomeric excesses generally approach or exceed known cases.